US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Oct 28, 2025 (10 months ago)

Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

What was recalled

Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0

Recalling firm
Agebox
Origin
DE, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0344-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.